Hi. My mom is 71 and has dementia. Its gotten must worse in the past 12 months and my Dad can no longer take care of her on his own.
She no longer recognizes Dad as her husband but thinks he's a distant relative who lives with her. We need to separate them as he has major burn-out and we are worried for his health also.
She also has anosognosia which means she doesn't realize anything is wrong and believes she is perfectly fine to take care of herself.
She becomes extremely angry and leaves the room anytime we bring up a care home. She says she is fine to take care of herself, that nothing is wrong, and that she's not ready to go to a home. She thinks all care homes are essentially for people who can't take care of themselves or hospices where old people go to die. She won't even consider touring a retirement or assisted living home to see that they are actually very nice places.
We have power-of-attorney and could force her... but I think we would physically need to tie her up to get her through the door. I don't want it to be traumatic.
We're thinking of maybe turning the water off and saying the water in the house froze due to the recent very cold weather...
Any suggestion on how do we get her into a care home?
If she does have a diagnosis then employing an "therapeutic fib" like you suggested is perfectly acceptable. I would stop trying to get her buy-in into transitioning into a facility...it's never going to happen. Tell her the pipes froze or there is a mold or insect infestation that requires everyone to vacate the home for a week. Resettle her into MC care on the pretense it is the "hotel". Make sure the facility is in on this ruse (they will be happy to go along).
Is it possible to hire some outside agency help to manage her/be a companion to her during the day? Or adult daycare? None of this will feel good or easy, but it sounds like it is necessary. All you can do is what is in her own best interests and what doesn't burn out the other caregivers. May you gain peace in your heart about this decision.
You might want to double check the document AND the attorney who drew up the POA. Our mother, despite having AL in her plans before dementia kicked in, refused to consider moving anywhere, ESP not AL. Our attorney told me we could NOT force her to move, and suggested guardianship. I don't think she would have qualified for guardianship at that time, or perhaps a minimal level (I didn't know there were possible "levels", but Bab75 was granted SOME guardianship), but it was a moot point anyway, because the facility we chose would not accept a committal. In order to make the move happen, we had to come up with a plausible fib/scenario that she would buy into. Similar to what you and Geaton777 suggested.
This
https://www.agingcare.com/articles/things-you-can-and-cant-do-with-poa-152673.htm
spells out a number of things you can/can't do with medical or financial POAs, but basically a POA is giving you the ability to perform certain duties AS that person, in their stead. It can allow certain decisions to be made if the person isn't capable, but before assuming this also allows you to force a move, you need to double check with the attorney. The article doesn't mention moving.
Even staff in the MC unit told me they can't force residents to do anything they say no to, such as taking their meds, bathing, getting medical/wound treatment. They have to become adept at coaxing the person, working to get them to agree.
Shutting off the water might be a way to move her, saying it's temporary. Once in the MC unit, it should be sufficiently locked that no one leaves without staff allowing it. Do NOT try AL - they don't "watch" over them, so she could walk out at any time! I had suggested my brother mess with the Nest thermostat he installed - make it way too hot, then too cold, and tell her it needs to be replaced and will take some time (it was already into winter.) She injured her leg just before the move, developed cellulitis, which delayed the move a few days, but he used that to draft up a fake letter from 'Elder Services' telling her she moves to where we pick or they will pick. Thankfully it worked (but, funny note - not long after, when going there to work on clearing, cleaning and repairing, to sell it, the heating system DID die!)
Maybe, if possible, work with the place you choose and see if dad can move in with her, briefly at least, just to keep the hotel "ruse" up. Explain the unit lock is to keep infected OR bad people out. Have him leave, as if going to work on fixing the problem during the day. Eventually, given a little time, he can return home and visit during the day. She may also need some meds, to calm any anxiety during the transition. They did that for my mother - minimal dose, just to take the edge off. It was used later, when she had a UTI with major sun-downing, so I know she wasn't "doped up."
Never heard the term before, but it does seem that most people with dementia think they are fine. Part of that is due to short term memory loss. They are seeing themselves as they were several years ago, still healthy and capable! Mom was certainly adamant there wasn't anything wrong with her! I'm Fine. I'm Independent. I can cook. Nope. Nope. Nope. I also never used the "D" word around her. She might acknowledge forgetting some things, but wrote that off as she's "old and entitled to forget once in a while!" As she moved back in time, she thought a pic of herself was her mother. Self-image does change.
Another option, for getting her to see these places aren't what many remember from long ago is to schedule a meal with them (when allowed) and pretend you're going to a restaurant. When done, amble around (with a tour guide) to see the place. Mom actually thought the place was nice, but asked who's going to pay for it. I just said VA (long story, didn't pan out, but they don't cover that much!) By the time she was home, she'd forgotten why we were even there!
My husband and I went through the same thing with my MIL but she lived alone. We resorted to lying to her to get her to the facility. Yes, she was initially upset, but within a few days she was very happy to be in her new home and never mentioned “going home” again. You need to take control of a bad situation similar to when you need to make decisions for young children.
I do understand your situation is totally different - just a thought. Don't beat yourself up. It's a hard road with no easy answers. Good luck.
First off, make sure you have ALL your ducks in a row!!
Read the POA very carefully!
Do you have a diagnosis from a Geriatrician or Neurologist?
Perhaps speak with an elder care attorney.
We told my Aunt (Alzheimer's), that her home needed repairs and she needed to stay elsewhere while it was going on.
Although she still tells me periodically that she's going home tomorrow, she has no idea how long she's been in memory care. It took a little while, but she has settled in nicely.
I thought about cameras etc..., but after witnessing her start kitchen fires twice, I knew that wasn't a plausible idea in her case.
You'll get lots of advice pro and con ALFs! Only you know what the best option is for your parents!
There is no shame in placing LOs in ALF or trying to keep them at home.
Your local Council on Aging may also be able to give you sound advice.
Best wishes!!!
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